TCI C0623 Cyclooctanol is a secondary alcohol built on a medium-sized eight-membered ring. Its hydroxyl group readily undergoes oxidation, esterification, etherification, and conversion into leaving groups, with oxidation to cyclooctanone being a particularly common route. The distinctive conformational behaviour of the eight-membered ring also makes it useful for studying ring-size effects on reactivity. Supplied in a 25 g pack, it should be handled in a well-ventilated area and stored cool, dry, and away from strong oxidising agents.
Related TCI products
- TCI C4056 27607-33-6 cis-Cyclooctane-1,2-diol
- TCI E0516 286-62-4 1,2-Epoxycyclooctane
- TCI D2910 108249-93-0 2,8-Dichlorocyclooctanone
- TCI C0504 502-49-8 Cyclooctanone
- TCI C0501 292-64-8 Cyclooctane
- TCI C0503 111-78-4 1,5-Cyclooctadiene [stabilized with Octadecyl 3-(3',5'-Di-tert-butyl-4'-hydroxyphenyl)propionate]
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- Andersson et al. (1990). Thermal conductivity, heat capacity and phase diagram of cyclooctanol in liquid, solid and glassy crystal states under high pressure. Molecular Physics doi:10.1080/00268979000101951
- Ściesiński et al. (1995). Calorimetric study of cyclooctanol. Phase Transitions doi:10.1080/01411599508200401
- Khan et al. (1997). A Novel Sm(II)-Induced Route to Highly Substituted Benzannulated Cyclooctanol Derivatives. Synlett doi:10.1055/s-1997-934
References were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.






![1,5-Cyclooctadiene [stabilized with Octadecyl 3-(3',5'-Di-tert-butyl-4'-hydroxyphenyl)propionate] (CAS 111-78-4) - TCI C0503 - AMI Scientific](http://amiscientific.com/cdn/shop/files/TCI2510C0503.jpg?v=1767095399&width=533)
